RAD21 Mutations Cause a Human Cohesinopathy-Reference-Cited by-同舟云学术

RAD21 Mutations Cause a Human Cohesinopathy

Published:2012-06 Issue:6 Volume:90 Page:1014-1027
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Deardorff Matthew A.,Wilde Jonathan J.,Albrecht Melanie,Dickinson Emma,Tennstedt Stephanie,Braunholz Diana,Mönnich Maren,Yan Yuqian,Xu Weizhen,Gil-Rodríguez María Concepcion,Clark Dinah,Hakonarson Hakon,Halbach Sara,Michelis Laura Daniela,Rampuria Abhinav,Rossier Eva,Spranger Stephanie,Van Maldergem Lionel,Lynch Sally Ann,Gillessen-Kaesbach Gabriele,Lüdecke Hermann-Josef,Ramsay Robert G.,McKay Michael J.,Krantz Ian D.,Xu Huiling,Horsfield Julia A.,Kaiser Frank J.

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference69 articles.

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2. Releasing cohesin from chromosome arms in early mitosis: Opposing actions of Wapl-Pds5 and Sgo1;Shintomi;Genes Dev.,2009

3. Human Scc4 is required for cohesin binding to chromatin, sister-chromatid cohesion, and mitotic progression;Watrin;Curr. Biol.,2006

4. Two human orthologues of Eco1/Ctf7 acetyltransferases are both required for proper sister-chromatid cohesion;Hou;Mol. Biol. Cell,2005

5. Cohesins form chromosomal cis-interactions at the developmentally regulated IFNG locus;Hadjur;Nature,2009

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